Fluoroquinolone-Resistant Escherichia coli | CDC EID

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Volume 16, Number 1–January 2010
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Broiler Chickens as Source of Human Fluoroquinolone-Resistant Escherichia coli, Iceland
Thorunn R. Thorsteinsdottir, Gunnsteinn Haraldsson, Vala Fridriksdottir, Karl G. Kristinsson, and Eggert Gunnarsson
Author affiliations: University of Iceland, Reykjavík, Iceland (T.R. Thorsteinsdottir, G. Harladsson, V. Fridriksdottir, K.G. Kristinsson, E. Gunnarsson); and Landspitali University Hospital, Reykjavík (G. Haraldsson, K.G. Kristinsson)

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Abstract
To investigate feed as a source for fluoroquinolone-resistant Escherichia coli in broiler chickens, we compared antimicrobial drug–resistant E. coli from broiler feed and broilers with ciprofloxacin-resistant human clinical isolates by using pulsed-field gel electrophoresis. Feed was implicated as a source for ciprofloxacin-resistant broiler-derived E. coli and broilers as a source for ciprofloxacin-resistant human-derived E. coli.

In a previous study, we found a relatively high prevalence of antimicrobial and especially quinolone resistance among Escherichia coli isolates from broiler chickens and broiler meat (1), despite no known antimicrobial drug selection pressure in chicken farming in Iceland and biosecurity measures to prevent transmission of infectious agents into farms. Broiler houses are cleaned and disinfected after broiler flocks are transported to slaughter. Therefore, resistant bacteria are unlikely to persist in the broiler houses. However, animal feed can be contaminated with antimicrobial drug–resistant E. coli (2).

The high prevalence of quinolone-resistant E. coli isolates obtained from broilers and broiler meat coincides with an increasing prevalence of fluoroquinolone resistance among human clinical E. coli isolates in Iceland. This increase correlated with increased use of fluoroquinolones in clinical settings (3).

We examined whether the prevalence of resistant E. coli strains in broilers had changed since our previous study and whether broiler feed could be a source for the resistant strains. Furthermore, we compared the genotypes of ciprofloxacin-resistant broiler, broiler meat, and broiler feed E. coli isolates with ciprofloxacin-resistant human clinical E. coli isolates.

The Study
The sampling period for this study was May through November 2008. Pooled cecal samples (20 ceca from each flock) were taken from the 30 flocks slaughtered at all 3 broiler slaughterhouses in Iceland in June 2008. Ceca were stomachered in phosphate-buffered saline, spread on MacConkey agar with and without enrofloxacin (0.25 mg/L), and incubated overnight. Feed was sampled from feed stalls at 18 farms (of which 14 had participated in the previous study) and from 2 feed mills; the feed was suspended in buffered peptone water, mixed, incubated overnight, and spread on MacConkey agar as described above. One colony from each agar plate was selected for susceptibility testing as described in our previous study (1). Because isolates were collected from the 18 largest broiler farms (of the 27 farms operating in Iceland), all the broiler slaughterhouses, and the only 2 feed mills operating in Iceland, we believe this study provides a representative sample.

We selected all 34 available human E. coli isolates recovered from routine clinical specimens (mostly urine and blood) at the main clinical microbiology/reference laboratory in Iceland (Landspitali University Hospital) during 2006–2007, which had similar susceptibility patterns to the strains previously isolated from broilers (1) (ampicillin-tetracycline-sulfamethoxazole/trimethoprim-ciprofloxacin or ciprofloxacin alone). Only 1 isolate was chosen from each patient.

We performed susceptibility testing using a microbroth dilution method (VetMIC; National Veterinary Institute, Uppsala, Sweden). MICs were determined for ampicillin, cefotaxime, ceftiofur, chloramphenicol, ciprofloxacin, florfenicol, gentamicin, nalidixic acid, kanamycin, streptomycin, sulfamethoxazole, tetracycline, and trimethoprim. Cutoff values were those used in the monitoring programs in Sweden and Norway (4,5). Strains resistant to >3 classes of antimicrobial agents were considered multiresistant.

We compared all E. coli broiler ceca and feed isolates resistant to >1 antimicrobial agents and the 34 ciprofloxacin-resistant human E. coli isolates with resistant E. coli isolates from the previous study (2005–2007) (1) by pulsed-field gel electrophoresis (PFGE) using a slightly modified method of Ribot et al. (6). Comparison of PFGE patterns was made by visual inspection and BioNumerics software (Applied Maths, Sint-Martens-Latem, Belgium). For cluster analysis, the Dice coefficient for band matching (band-position tolerance 1.5%) was used to generate an unweighted pair group method with arithmetic averages dendrogram. Isolates from the previous and present study that did not yield a satisfactory banding pattern by PFGE were genotyped by randomly amplified polymorphic DNA (RAPD) analysis as described (7). Reaction products were analyzed by electrophoresis on 1.5% agarose gels stained with ethidium bromide. Patterns were considered different when the profiles differed by at least 1 band. Similarity among RAPD patterns was compared as described for PFGE. Clusters for PFGE and composite RAPD profiles were defined as >2 isolates with >80% similarity. Prevalence values were compared by using the Fisher exact test.

Of the 40 broiler isolates, 20 were resistant to >1 of the antimicrobial drugs tested (Table); only 1 was multidrug resistant (resistant to streptomycin, tetracyclin, sulfamethoxazole, and trimethoprim). Ciprofloxacin and nalidixic acid were always cross-resistant. Compared with the previous sampling, the prevalence of resistance increased significantly for ciprofloxacin and nalidixic acid (from 18.2% to 42.5%; p<0.0001) but decreased significantly for ampicillin (from 18.2% to 0.0%; p = 0.002) and sulfamethoxazole (from 19.1% to 5.0%; p = 0.0398). This finding suggests that quinolone resistance was not transferred with resistance to the other antimicrobial agents and that it was selected for by other factors. Of the 22 E. coli isolates obtained from feed, 7 (32%) were resistant to ciprofloxacin and nalidixic acid, and all were susceptible to the other antimicrobial agents tested. Although no E. coli were isolated from the 2 feed mill samples, other Enterobacteriaceae grew on the agar plates, which could have overgrown existing E. coli strains, if any, demonstrating that the feed was not sterile.

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